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Cancer Science|August 7, 2019
Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndromeYasuo Kubota, Kumiko Uryu, Tatsuya Ito, et al.Rheumatology (Oxford, England)|November 4, 2023
Real-world comparative study of the efficacy of Janus kinase inhibitors in patients with rheumatoid arthritis: the ANSWER cohort studyShinya Hayashi, Shotaro Tachibana, Toshihisa Maeda, et al.American Journal of Human Genetics|November 12, 2013
Mutations in SERPINB7, encoding a member of the serine protease inhibitor superfamily, cause Nagashima-type palmoplantar keratosisAkiharu Kubo, Aiko Shiohama, Takashi Sasaki, et al.Nature Genetics|May 7, 2024
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalitiesSatoshi Narumi, Keisuke Nagasaki, Mitsuo Kiriya, et al.Plos One|December 18, 2018
Familial episodic limb pain in kindreds with novel Nav1.9 mutationsRisako Kabata, Hiroko Okuda, Atsuko Noguchi, et al.Allergy|August 17, 2021
Direct platelet adhesion potentiates group 2 innate lymphoid cell functionsKeisuke Orimo, Masato Tamari, Tomohiro Takeda, et al.Development (Cambridge, England)|May 23, 2014
DNMT3L promotes quiescence in postnatal spermatogonial progenitor cellsHung-Fu Liao, Wendy S C Chen, Yu-Hsiang Chen, et al.Journal of Human Genetics|February 26, 2016
Human genetic variation database, a reference database of genetic variations in the Japanese populationKoichiro Higasa, Noriko Miyake, Jun Yoshimura, et al.Cancer Research|June 21, 2018
Recurrent <i>RARB</i> Translocations in Acute Promyelocytic Leukemia Lacking <i>RARA</i> TranslocationTomoo Osumi, Shin-Ichi Tsujimoto, Moe Tamura, et al.Plos Genetics|December 7, 2023
Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysisYosuke Kawai, Yusuke Watanabe, Yosuke Omae, et al.Pageof 27